Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAAACTGCTGACGATGCAGAGTTCC[C/G]TGACGGTGCAGGAAGGCCTGTGTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605640 | ||||||||||||||||||||
Literature Links: |
SIGLEC9 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SIGLEC9 - sialic acid binding Ig like lectin 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198558.1 | 152 | Missense Mutation | CTG,GTG | L,V 29 | NP_001185487.1 | |
NM_014441.2 | 152 | Missense Mutation | CTG,GTG | L,V 29 | NP_055256.1 | |
XM_006723146.3 | 152 | Missense Mutation | CTG,GTG | L,V 29 | XP_006723209.1 | |
XM_011526730.2 | 152 | Missense Mutation | CTG,GTG | L,V 29 | XP_011525032.1 | |
XM_011526732.2 | 152 | Missense Mutation | CTG,GTG | L,V 29 | XP_011525034.1 | |
XM_017026595.1 | 152 | Missense Mutation | CTG,GTG | L,V 29 | XP_016882084.1 | |
XM_017026596.1 | 152 | Missense Mutation | CTG,GTG | L,V 29 | XP_016882085.1 |